1,721,031 research outputs found
Mongelli, G., Boni, M., Buccione, R., Mameli, P., Mondillo, N., Oggiano, G., Sinisi, R., 2016 Critical metals distribution in Tethyan karst bauxite: the Cretaceous Italian example. Rend. Online Soc. Geol. It., Suppl. n. 1 al Vol. 40. September Napoli, 7-9, 2016.
Spatial distribution of rock uplift in the Bongarà district (Peruvian Andes) and implications for the genesis of supergene ore deposits
Topography and river landscape morphometry of two hydrographic basins, the Utcubamba River and the Chiriaco River basins (Bongará district, Amazonas region) allowed to determine the relationship between the irregular distribution of vertical motions (e.g., rock uplift) and the genesis of supergene Zn deposits. The latter derives from variable weathering of pre-existing carbonate-hosted Zn sulfides orebodies, in three distinct localities: Florida Canyon, Mina Grande and Cristal. The research was carried out through the evaluation of the parameters such as elevation, local relief, swath profile, river longitudinal profiles and transformed river profiles (χ-long profiles), and slope/area analysis to derive the normalized channel steepness index (ksn). The NE-ward sharp increase in mean and minimum elevation coupled with a jump in the mean ksn values, suggests that the Chiriaco River basin has experienced more recent rock uplift than the Utcubamba River basin. In fact, the Utcubamba River experienced a long-lasting uplift, resulting in a rugged local relief and lowering the mean and minimum elevations, and exhumation and weathering of the Triassic-hosted sulfide mineral deposits at Florida Canyon. In the Chiriaco River basin, the younger uplift has promoted the weathering of the more surficial Jurassic-hosted Mina Grande and Cristal mineral deposits. The morphometric approach proved to be effective in recognizing fertile areas with near-surface orebodies also in regions characterized by distinct types of ore deposits
The mineralogy and geochemistry of the Pirashkaft bauxite, Zagros belt, Iran: New inferences on the paleo-climate at the time of formation and on the nature of the parent rock
The Pirashkaft karst type bauxite is located in north of the Paskuhak anticline, Pirashkaft region, in the Fars province (Iran). The deposit is composed of six bauxite horizons, occurring between upper Cretaceous Sarvak and Gurpy Formations, and formed in the late Turonian. Mineralogical composition includes boehmite, hematite, diaspore, kaolinite, goethite, anatase and minor minerals like, gibbsite, spinel, rutile, and kaolinite. The major oxides in the bauxite horizons mainly comprise Al2O3 (46.93–61.34 wt%), SiO2 (5.78–14.60 wt%), Fe2O3 (11.22–28.00 wt%), and TiO2 (1.66–3.03 wt%). The bauxite has a pisolitic–oolitic texture. Pisoids are mainly composed of large Al-bearing hematite cores, surrounded by layers of gibbsite or boehmite. This structure suggests that bauxite formed under a humid climatic regime, punctuated by periodic arid periods. In the Pirashkaft deposit, LREEs vary between 136.49 ppm and 928.56 ppm, whilst HREEs range from 16.48 ppm to 59.5 ppm. Positive anomalies of Ce (Ce/Ce* between 1.08 and 2.36) indicate dominant oxidizing conditions during the bauxitization process. The Eu/Eu* anomalies of the bauxite samples vary between 0.44 and 0.92, this suggesting that parent material likely derived from two geochemically distinct source rocks. Stratigraphical, mineralogical, and geochemical evidences, such as the REE distribution between the bauxitic horizons and the Sarvak marly limestone, suggest that the underlying marly carbonates were one of the sources of the Pirashkaft bauxite
Ni-bearing smectites in the Wingellina laterite deposit (Western Australia) at nanoscale: TEM-HRTEM evidences of the formation mechanisms
Ni-bearing clays represent the main ore minerals in many laterite districts. Although the world-class Wingellina deposit (Western Australia) is an oxide-dominated ore, about 30% of the total Ni resources are hosted in the saprolitic section of the tenure, making the Ni-bearing clays a strategic target to increase the future ore reserves. In this study we present a detailed micro- to nanotextural TEM-HRTEM investigation of Ni-bearing smectites, which at Wingellina represent the main mineralogical species in the phyllosilicates assemblage. Ni-bearing smectites belong mainly to the dioctahedral (i.e. montmorillonite and nontronite) and to the trioctahedral (saponite and ferrosaponite) groups. The nanoscale TEM-HRTEM imaging indicates that Ni-bearing clays occur either as a replacement of the former clay suite (i.e. polygonal serpentine and chlorite) or as porous clay aggregates (i.e. PCA). Most of PCA was found closely associated with nanometric Co-bearing Mn-oxy-hydroxides. This finding not only provides a better understanding of the early stage formation of Mn-oxy-hydroxides in laterite systems, but is also important to better constrain the Co distribution and targeting within unconventional laterite ore facies. The nanoscale HRTEM imaging coupled with SAED allowed detecting minor Ni-bearing chlorite amounts, which were not found through previous XRPD-based techniques. Moreover, the paragenetic association of chlorite with primary serpentine suggests a pre-lateritic formation for chlorite. The detection of Ni-bearing trioctahedral smectite as alteration product of primary chlorite is of relevant importance, as it fills a gap in the knowledge of ore-formation processes occurring in smectite-endowed laterites
Influence of genetic processes on geochemistry of fe-oxy-hydroxides in supergene Zn non-sulfide deposits
In supergene Zn non-sulfide deposits, the Fe-oxy-hydroxides (FeO/OH) are mainly concentrated in the residual zones (gossan) on top of the oxidized ore bodies, although they can also be found throughout the whole weathering profile coexisting with the primary and secondary ore assemblages. Fe-oxy-hydroxides are rarely pure as they form in systems where a wide range of metals, most of them of economic importance (e.g., Zn, Pb, Co, REE, Sc, Ga, Ge, V, etc.), freely circulate and can be “captured” under specific conditions. Although their occurrence can be widespread, and they have a potential to scavenge and accumulate critical metals, FeO/OH are considered gangue phases during the existing processing routes of Zn non-sulfide ores. Moreover, very little is known about the role of the deposit type on the geochemistry of FeO/OH formed in a specific association. Therefore, this paper provides a comprehensive assessment of the trace element footprint of FeO/OH from a number of Zn non-sulfide deposits, in order to define parameters controlling the metals’ enrichment process in the mineral phase. To achieve this, we selected FeO/OH-bearing mineralized samples from four supergene Zn non-sulfide ores in diverse settings, namely Hakkari (Turkey), Jabali (Yemen), Cristal (Peru) and Kabwe (Zambia). The petrography of FeO/OH was investigated by means of scanning electron microscope energy dispersive analysis (SEM-EDS), while the trace element composition was assessed using laser ablation-ICP-MS (LA-ICP-MS). Statistical analyses performed on LA-ICP-MS data defined several interelement associations, which can be ascribed to the different nature of the studied deposits, the dominant ore-formation process and subsequent evolution of the deposits and the environmental conditions under which FeO/OH phases were formed. Based on our results, the main new inferences are: (A) Zinc, Si, Pb, Ga and Ge enrichment in FeO/OH is favored in ores where the direct replacement of sulfides is the dominant process and/or where the pyrite is abundant (e.g., Cristal and Hakkari). (B) When the dissolution of the host-rock is a key process during the supergene ore formation (i.e., Jabali), the buffering toward basic pH of the solutions favors the uptake in FeO/OH of elements leached from the host carbonate rock (i.e., Mn), whilst restricting the uptake of elements derived from the dissolution of sulfides (i.e., Zn, Pb, Ga and Ge), as well as silica. (C) The input of exotic phases can produce significant enrichment in “unconventional” metals in FeO/OH (i.e., Cr and Co at Kabwe; Y at Cristal) depending on whether the optimal pH-Eh conditions are attained. (D) In the Kabwe deposit, FeO/OH records heterogeneous geochemical conditions within the system: where locally basic conditions prevailed during the alteration process, the V and U concentration in FeO/OH is favored; yet conversely, more acidic weathering produced Zn-and Si-bearing FeO/OH
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